ABO blood groups in humans are controlled by the gene I. It has three alleles – IA IB and i. Since there are three different alleles, six different genotypes are possible. How many phenotypes can occur?

1. Three

2. One

3. Four

4. Two

Subtopic:  Dominance Deviation from Mendel: 2 |
 83%
From NCERT
AIPMT - 2010
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Select the correct statement from the ones given below with respect to dihybrid cross:

1. Tightly linked genes on the same chromosome show higher recombinations
2. Genes far apart, on the same chromosome, show very few recombinations
3. Genes loosely linked, on the same chromosome, show similar recombinations as the tightly linked ones
4. Tightly linked genes on the same chromosome show very few recombinations

Subtopic:  Dihybrid Cross Analysis |
 81%
From NCERT
AIPMT - 2010
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Sickle cell anaemia is:

1. an autosomal linked dominant trait
2. caused by substitution of valine by glutamic acid
in the globin chain of haemoglobin
3. caused by a change in base pair of DNA
4. characterized by elongated sickle like RBCs with
a nucleus

Subtopic:  Mendelian Disorders: Sickle Cell Anemia |
 52%
From NCERT
AIPMT - 2009
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Point mutation involves:

1. insertion

2. change in single base pair

3. duplication 

4. deletion

Subtopic:  Mutation |
 92%
From NCERT
AIPMT - 2009
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Study the pedigree chart given below:



What does it show?

1. Inheritance of a sex-linked inborn error of metabolism
2. Inheritance of a condition like phenylketonuria as an
autosomal recessive trait
3. The pedigree chart is wrong as this is not possible
4. Inheritance of a recessive sex-linked disease like
haemophilia

Subtopic:  Pedigree Analysis: Problem Solving | Mendelian Disorders |
 77%
From NCERT
AIPMT - 2009
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Which one of the following conditions in humans is correctly matched with its chromosomal abnormality/linkage?
1. Klinefelter's syndrome-44 autosomes + XXY
2. Colourblindness – Y-linked
3. Erythroblastosis foetalis-- X-linked
4. Down syndrome--44 autosomes + XO
Subtopic:  Sex Aneuploidy - Turner & Klinefelter Syndrome |
 85%
From NCERT
AIPMT - 2008
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Inheritance of skin colour in humans is an example of:

1. chromosomal aberration

2. point mutation

3. polygenic inheritance

4. codominance

Subtopic:  Polygenic Inheritance & Pleiotropy |
 92%
From NCERT
AIPMT - 2007
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Two genes R and Y are located very close on the chromosomal linkage map of the maize plant. When RRYY and rryy genotypes are hybridized, then F2 segregation will show:

1. higher number of the recombinant types

2. segregation in the expected 9:3:3:1 ratio

3. segregation in a 3:1 ratio

4. higher number of the parental types

Subtopic:  Dihybrid Cross Analysis | Dihybrid Cross: Details |
 60%
From NCERT
AIPMT - 2007
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A common test to find the genotype of a hybrid is by:

1. crossing of one F2 progeny with a male parent

2. crossing of one F2 progeny with a female parent

3. studying the sexual behaviour of F1 progenies

4. crossing of one F1 progeny with a male parent

Subtopic:  Monohybrid Cross: Further Understanding |
From NCERT
AIPMT - 2007
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In pea plants, yellow seeds are dominant to green. If a heterozygous yellow-seeded plant is crossed with a green-seeded plant, what ratio of yellow and green-seeded plants would you expect in F1generation?

1. 50:50

2. 9:1

3. 1:3

4. 3:1

Subtopic:  Monohybrid Cross: Further Understanding |
 72%
From NCERT
AIPMT - 2007
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